Variant report

Variant	nsv873352
Chromosome Location	chr1:239755406-239798412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:239797470-239797513	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr1:239780047-239780400	A549	lung:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
3	CEBPB	chr1:239768488-239768747	HepG2	liver:	n/a	n/a
4	CEBPB	chr1:239779848-239780403	MCF-7	breast:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779960-239779971 chr1:239779994-239780006 chr1:239779994-239780007
5	CEBPB	chr1:239779942-239780432	MCF-7	breast:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779960-239779971 chr1:239779994-239780006 chr1:239779994-239780007
6	CEBPB	chr1:239780008-239780303	A549	lung:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
7	CEBPB	chr1:239780000-239780328	HepG2	liver:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183
8	CEBPB	chr1:239779986-239780373	Hela-S3	cervix:	n/a	chr1:239780173-239780182 chr1:239780088-239780101 chr1:239780171-239780182 chr1:239780172-239780183 chr1:239779994-239780006 chr1:239779994-239780007
9	CEBPB	chr1:239756265-239756339	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:239768485-239768778	IMR90	lung:	n/a	n/a
11	CEBPB	chr1:239766207-239766366	IMR90	lung:	n/a	n/a
12	CTCF	chr1:239776156-239776179	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:239776136-239776156	Lung_OC	lung:	n/a	n/a
14	CTCF	chr1:239774000-239774150	HEK293	kidney:	n/a	n/a
15	E2F4	chr1:239766845-239767193	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr1:239765657-239765839	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr1:239770623-239770786	GM12878	blood:	n/a	chr1:239770768-239770778 chr1:239770769-239770778 chr1:239770767-239770780 chr1:239770769-239770779
18	EGR1	chr1:239766891-239767152	MCF-7	breast:	n/a	chr1:239767041-239767051 chr1:239767039-239767052 chr1:239767041-239767051 chr1:239767040-239767051 chr1:239767042-239767051 chr1:239767038-239767053 chr1:239767040-239767051 chr1:239767039-239767053 chr1:239767035-239767057 chr1:239767039-239767052 chr1:239767041-239767050
19	EGR1	chr1:239766946-239767236	ECC-1	luminal epithelium:	n/a	chr1:239767041-239767051 chr1:239767039-239767052 chr1:239767041-239767051 chr1:239767040-239767051 chr1:239767042-239767051 chr1:239767038-239767053 chr1:239767040-239767051 chr1:239767039-239767053 chr1:239767035-239767057 chr1:239767039-239767052 chr1:239767041-239767050
20	EP300	chr1:239756973-239757192	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr1:239758959-239759032	GM12878	blood:	n/a	n/a
22	FOS	chr1:239766813-239767306	MCF10A-Er-Src	breast:	n/a	chr1:239767029-239767037 chr1:239767030-239767037 chr1:239767029-239767037 chr1:239767028-239767038
23	FOS	chr1:239770430-239770630	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr1:239770446-239770625	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr1:239780005-239780344	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:239766855-239767191	MCF10A-Er-Src	breast:	n/a	chr1:239767029-239767037 chr1:239767030-239767037 chr1:239767029-239767037 chr1:239767028-239767038
27	FOS	chr1:239779976-239780352	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:239780001-239780327	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:239779995-239780365	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:239766852-239767215	MCF10A-Er-Src	breast:	n/a	chr1:239767029-239767037 chr1:239767030-239767037 chr1:239767029-239767037 chr1:239767028-239767038
31	FOS	chr1:239766851-239767223	MCF10A-Er-Src	breast:	n/a	chr1:239767029-239767037 chr1:239767030-239767037 chr1:239767029-239767037 chr1:239767028-239767038
32	FOSL2	chr1:239779963-239780353	MCF-7	breast:	n/a	n/a
33	FOSL2	chr1:239779912-239780331	MCF-7	breast:	n/a	n/a
34	FOXA2	chr1:239792013-239792708	A549	lung:	n/a	n/a
35	FOXA2	chr1:239792144-239792578	A549	lung:	n/a	n/a
36	GATA2	chr1:239756854-239757184	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr1:239779853-239780387	SK-N-SH	brain:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
38	GATA3	chr1:239756830-239757228	MCF-7	breast:	n/a	n/a
39	GATA3	chr1:239756789-239757226	T-47D	breast:	n/a	n/a
40	GATA3	chr1:239779853-239780437	MCF-7	breast:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
41	GATA3	chr1:239758934-239758941	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr1:239756373-239756594	SH-SY5Y	brain:	n/a	chr1:239756402-239756411
43	GATA3	chr1:239756812-239757336	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr1:239779973-239780394	SK-N-SH	brain:	n/a	chr1:239780127-239780143 chr1:239780134-239780141
45	GATA3	chr1:239775921-239775926	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr1:239779667-239780588	MCF-7	breast:	n/a	chr1:239780127-239780143 chr1:239779717-239779728 chr1:239780134-239780141
47	GATA3	chr1:239756771-239757183	T-47D	breast:	n/a	n/a
48	GATA3	chr1:239756671-239757305	MCF-7	breast:	n/a	n/a
49	GATA3	chr1:239766932-239767474	MCF-7	breast:	n/a	chr1:239767282-239767289 chr1:239767277-239767293 chr1:239767282-239767289 chr1:239767282-239767289 chr1:239767240-239767256 chr1:239767275-239767296
50	KAP1	chr1:239756029-239757167	U2OS	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:239792663-239792713	RPTEC	kidney:	n/a
2	chr1:239792663-239792713	MCF10A-Er-Src	breast:	n/a
3	chr1:239792663-239792713	A549	lung:	n/a
4	chr1:239792663-239792713	T-47D	breast:	n/a
5	chr1:239792663-239792713	NH-A	brain:	n/a
6	chr1:239792663-239792713	HRCEpiC	kidney:	n/a
7	chr1:239792663-239792713	GM12878	blood:	n/a
8	chr1:239792663-239792713	NHBE	bronchial:	n/a
9	chr1:239792663-239792713	Caco-2	colon:	n/a
10	chr1:239792663-239792713	HCT-116	colon:	n/a
11	chr1:239792663-239792713	HEK293	kidney:	embryo
12	chr1:239792663-239792713	SK-N-SH_RA	brain:	n/a
13	chr1:239792663-239792713	AG04449	skin:	fetal
14	chr1:239792663-239792713	BJ	skin:	n/a
15	chr1:239792663-239792713	BE2_C	brain:	n/a
16	chr1:239792663-239792713	GM12891	blood:	n/a
17	chr1:239792663-239792713	HCPEpiC	choroid plexus:	n/a
18	chr1:239792663-239792713	SKMC	muscle:	n/a
19	chr1:239792663-239792713	HL-60	blood:	n/a
20	chr1:239792663-239792713	Hela-S3	cervix:	n/a
21	chr1:239792663-239792713	ovcar-3	ovarian:	n/a
22	chr1:239792663-239792713	SAEC	small airway:	n/a
23	chr1:239792663-239792713	PrEC	prostate:	n/a
24	chr1:239792663-239792713	HCM	heart:	n/a
25	chr1:239792663-239792713	HIPEpiC	eye:	n/a
26	chr1:239792663-239792713	Hepatocyte	liver:	n/a
27	chr1:239792663-239792713	HUVEC	blood vessel:	n/a
28	chr1:239792663-239792713	AG09319	gingival:	n/a
29	chr1:239792663-239792713	MCF-7	breast:	n/a
30	chr1:239792663-239792713	HCF	heart:	n/a
31	chr1:239792663-239792713	HAEpiC	amniotic membrane:	n/a
32	chr1:239792663-239792713	K562	blood:	n/a
33	chr1:239792663-239792713	PFSK-1	brain:	n/a
34	chr1:239792663-239792713	SK-N-SH	brain:	n/a
35	chr1:239792663-239792713	AoSMC	blood vessel:	n/a
36	chr1:239792663-239792713	ProgFib	skin:	n/a
37	chr1:239792663-239792713	CMK	blood:	n/a
38	chr1:239792663-239792713	HepG2	liver:	n/a
39	chr1:239792663-239792713	NHDF-neo	bronchial:	n/a
40	chr1:239792663-239792713	HPAEpiC	pulmonary alveolar:	n/a
41	chr1:239792663-239792713	U87	brain:	n/a
42	chr1:239792663-239792713	HEEpiC	esophagus:	n/a
43	chr1:239792663-239792713	HMEC	breast:	n/a
44	chr1:239792663-239792713	H1-hESC	embryonic stem cell:	embryo
45	chr1:239792663-239792713	GM19239	blood:	n/a
46	chr1:239792663-239792713	GM06990	blood:	n/a
47	chr1:239792663-239792713	Jurkat	blood:	n/a
48	chr1:239792663-239792713	LNCaP	prostate:	n/a
49	chr1:239792663-239792713	NT2-D1	testis:	n/a
50	chr1:239792663-239792713	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:239770818..239772337-chr1:239779962..239782828,2	MCF-7	breast:
2	chr1:239770818..239772337-chr1:239779962..239782828,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRM3-1	chr1:239795524-239795586	NONHSAT010470
2	lnc-CHRM3-1	chr1:239795551-239795576	NONHSAT010476
3	lnc-CHRM3-1	chr1:239769305-239769507	NONHSAT010472

Variant related genes	Relation type
CHRM3	TF binding region
CHRM3	CpG island

Extended variants
information (count: 1441 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1867262	chr1:239755406-239755407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188814243	chr1:239755408-239755409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544633488	chr1:239755431-239755432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116445869	chr1:239755451-239755452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560491677	chr1:239755478-239755479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200997456	chr1:239755535-239755536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373841961	chr1:239755579-239755580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181274707	chr1:239755586-239755587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185295267	chr1:239755624-239755625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529472198	chr1:239755633-239755634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549387726	chr1:239755676-239755677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548018143	chr1:239755729-239755730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12089818	chr1:239755735-239755736	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs535018486	chr1:239755773-239755774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12062962	chr1:239755779-239755780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188304738	chr1:239755785-239755786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575235392	chr1:239755815-239755816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537125068	chr1:239755850-239755851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374142140	chr1:239755956-239755957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180873170	chr1:239755963-239755964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567437419	chr1:239755978-239755979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534470818	chr1:239755996-239755997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565980524	chr1:239756001-239756002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553137069	chr1:239756002-239756003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368422500	chr1:239756026-239756027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187317458	chr1:239756034-239756035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538966904	chr1:239756078-239756079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556669785	chr1:239756153-239756154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192217312	chr1:239756166-239756167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542657399	chr1:239756201-239756202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141207515	chr1:239756237-239756238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs572975975	chr1:239756247-239756248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539217737	chr1:239756248-239756249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559936666	chr1:239756294-239756295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183699412	chr1:239756314-239756315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552080106	chr1:239756544-239756545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563848717	chr1:239756568-239756569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552281446	chr1:239756569-239756570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186177057	chr1:239756572-239756573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548975132	chr1:239756574-239756575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374886920	chr1:239756598-239756599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548998463	chr1:239756776-239756777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs202016548	chr1:239756781-239756782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567376234	chr1:239756782-239756783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79825976	chr1:239756790-239756791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77825158	chr1:239756791-239756792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575717932	chr1:239756861-239756862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190454947	chr1:239756887-239756888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543155936	chr1:239756894-239756895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555340203	chr1:239756927-239756928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:239728800-239769400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:239744000-239761400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr1:239746400-239756200	Weak transcription	Gastric	stomach
4	chr1:239746600-239757600	Weak transcription	Pancreas	Pancrea
5	chr1:239751000-239761200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:239752000-239757000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:239754600-239756200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:239754800-239757400	Weak transcription	Ovary	ovary
9	chr1:239755200-239755600	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr1:239755400-239756200	Weak transcription	Aorta	Aorta
11	chr1:239755400-239757000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:239755400-239761400	Weak transcription	Colon Smooth Muscle	Colon
13	chr1:239756000-239757200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr1:239756200-239756400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:239756200-239756400	Enhancers	Aorta	Aorta
16	chr1:239756200-239756400	Enhancers	Gastric	stomach
17	chr1:239756400-239756600	Weak transcription	Gastric	stomach
18	chr1:239757000-239757200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr1:239757000-239757800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:239760000-239760800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:239761200-239761600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:239761400-239761600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:239761400-239761600	Enhancers	Colon Smooth Muscle	Colon
24	chr1:239761400-239761800	Enhancers	Rectal Smooth Muscle	rectum
25	chr1:239770200-239771800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:239770400-239770600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr1:239770400-239770800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr1:239770600-239771600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr1:239771600-239772000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr1:239774000-239776000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:239775400-239776000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr1:239775800-239776000	Enhancers	Fetal Muscle Leg	muscle
33	chr1:239775800-239776200	Enhancers	Colon Smooth Muscle	Colon
34	chr1:239775800-239776200	Enhancers	Ovary	ovary
35	chr1:239775800-239776200	Enhancers	Stomach Smooth Muscle	stomach
36	chr1:239775800-239776400	Enhancers	Rectal Smooth Muscle	rectum
37	chr1:239776000-239780800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr1:239776000-239780800	Weak transcription	Fetal Muscle Leg	muscle
39	chr1:239779600-239780400	Enhancers	Hela-S3	cervix
40	chr1:239779600-239781800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:239779800-239781800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr1:239780800-239781400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr1:239780800-239781600	Enhancers	Primary hematopoietic stem cells	blood
44	chr1:239780800-239781800	Enhancers	Fetal Muscle Leg	muscle
45	chr1:239781000-239781600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr1:239781200-239781600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr1:239781200-239781600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:239781200-239781600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:239781200-239781600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr1:239781200-239781800	Enhancers	H1 Cell Line	embryonic stem cell

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